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Patrizia De Marco

Showing results (31-40 of 96) with videos related to

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Birth Defects Research. Part A, Clinical and Molecular Teratology|February 8, 2006
Mutational screening of the CYP26A1 gene in patients with caudal regression syndromePatrizia De Marco, Elisa Merello, Samantha Mascelli, et al.
Birth Defects Research|June 22, 2021
The first case of mosaic MNX1 mutation in an adult female with features of Currarino syndromeFerruccio Romano, Patrizia De Marco, Marzia Ognibene, et al.
Frontiers in Pediatrics|January 29, 2024
Abdominal rhabdoid tumor presenting with symptomatic spinal epidural compression in a newborn. A case reportShana Montalto, Michela Di Filippo, Valeria Capra, et al.
Human Molecular Genetics|August 16, 2011
Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humansJung Hwa Seo, Yulia Zilber, Sima Babayeva, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|February 25, 2006
HLXB9 homeobox gene and caudal regression syndromeElisa Merello, Patrizia De Marco, Samantha Mascelli, et al.
Birth Defects Research|July 17, 2025
Targeted Re-Sequencing of Neural Tube Defects Patients and Families Identifies Rare Variants in Genes Candidate From Animal ModelsFerruccio Romano, Patrizia De Marco, Marzia Ognibene, et al.
Journal of Molecular Neuroscience : MN|March 15, 2012
De novo MGC4607 gene heterozygous missense variants in a child with multiple cerebral cavernous malformationsLorena Mosca, Silvana Pileggi, Francesca Avemaria, et al.
Malaria Journal|June 3, 2026
Malignant malaria: autopsy findings and morphological featuresDaniele Colombo, Franca Del Nonno, Alessandra D'Abramo, et al.
Birth Defects Research|May 28, 2020
Sinus pericranii, skull defects, and structural brain anomalies in TRAF7-related disorderAndrea Accogli, Marcello Scala, Marco Pavanello, et al.
Human Mutation|September 9, 2011
Identification and characterization of novel rare mutations in the planar cell polarity gene PRICKLE1 in human neural tube defectsCiprian M Bosoi, Valeria Capra, Redouane Allache, et al.
Pageof 10

Showing results (31-40 of 96) with videos related to

Sort By:
Pageof 10
Birth Defects Research. Part A, Clinical and Molecular Teratology|February 8, 2006
Mutational screening of the CYP26A1 gene in patients with caudal regression syndromePatrizia De Marco, Elisa Merello, Samantha Mascelli, et al.
Birth Defects Research|June 22, 2021
The first case of mosaic MNX1 mutation in an adult female with features of Currarino syndromeFerruccio Romano, Patrizia De Marco, Marzia Ognibene, et al.
Frontiers in Pediatrics|January 29, 2024
Abdominal rhabdoid tumor presenting with symptomatic spinal epidural compression in a newborn. A case reportShana Montalto, Michela Di Filippo, Valeria Capra, et al.
Human Molecular Genetics|August 16, 2011
Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humansJung Hwa Seo, Yulia Zilber, Sima Babayeva, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|February 25, 2006
HLXB9 homeobox gene and caudal regression syndromeElisa Merello, Patrizia De Marco, Samantha Mascelli, et al.
Birth Defects Research|July 17, 2025
Targeted Re-Sequencing of Neural Tube Defects Patients and Families Identifies Rare Variants in Genes Candidate From Animal ModelsFerruccio Romano, Patrizia De Marco, Marzia Ognibene, et al.
Journal of Molecular Neuroscience : MN|March 15, 2012
De novo MGC4607 gene heterozygous missense variants in a child with multiple cerebral cavernous malformationsLorena Mosca, Silvana Pileggi, Francesca Avemaria, et al.
Malaria Journal|June 3, 2026
Malignant malaria: autopsy findings and morphological featuresDaniele Colombo, Franca Del Nonno, Alessandra D'Abramo, et al.
Birth Defects Research|May 28, 2020
Sinus pericranii, skull defects, and structural brain anomalies in TRAF7-related disorderAndrea Accogli, Marcello Scala, Marco Pavanello, et al.
Human Mutation|September 9, 2011
Identification and characterization of novel rare mutations in the planar cell polarity gene PRICKLE1 in human neural tube defectsCiprian M Bosoi, Valeria Capra, Redouane Allache, et al.
Pageof 10